N,N′-Bis[(E)-2,4,6-trimethyl­benzyl­idene]ethane-1,2-diamine

The title compound, C(22)H(28)N(2), which is a double imine derived from ethane-1,2-diamine and mesityl aldehyde, has crystallographic inversion symmetry, with both C=N bonds E configured. The dihedral angle between the mesityl ring system and the imide functional group is 23.89 (17)°.

Detalles Bibliográficos
Autores principales: Yumata, Nonzaliseko, Gerber, Thomas, Hosten, Eric, Betz, Richard
Formato: Online Artículo Texto
Lenguaje:English
Publicado: International Union of Crystallography 2011
Materias:
Organic Papers
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3213609/
https://www.ncbi.nlm.nih.gov/pubmed/22091186
http://dx.doi.org/10.1107/S1600536811029424
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author Yumata, Nonzaliseko
Gerber, Thomas
Hosten, Eric
Betz, Richard
author_facet Yumata, Nonzaliseko
Gerber, Thomas
Hosten, Eric
Betz, Richard
author_sort Yumata, Nonzaliseko
collection PubMed
description The title compound, C(22)H(28)N(2), which is a double imine derived from ethane-1,2-diamine and mesityl aldehyde, has crystallographic inversion symmetry, with both C=N bonds E configured. The dihedral angle between the mesityl ring system and the imide functional group is 23.89 (17)°.
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spelling pubmed-32136092011-11-16 N,N′-Bis[(E)-2,4,6-trimethyl­benzyl­idene]ethane-1,2-diamine Yumata, Nonzaliseko Gerber, Thomas Hosten, Eric Betz, Richard Acta Crystallogr Sect E Struct Rep Online Organic Papers The title compound, C(22)H(28)N(2), which is a double imine derived from ethane-1,2-diamine and mesityl aldehyde, has crystallographic inversion symmetry, with both C=N bonds E configured. The dihedral angle between the mesityl ring system and the imide functional group is 23.89 (17)°. International Union of Crystallography 2011-07-30 /pmc/articles/PMC3213609/ /pubmed/22091186 http://dx.doi.org/10.1107/S1600536811029424 Text en © Yumata et al. 2011 http://creativecommons.org/licenses/by/2.0/uk/ This is an open-access article distributed under the terms of the Creative Commons Attribution Licence, which permits unrestricted use, distribution, and reproduction in any medium, provided the original authors and source are cited.
spellingShingle Organic Papers
Yumata, Nonzaliseko
Gerber, Thomas
Hosten, Eric
Betz, Richard
N,N′-Bis[(E)-2,4,6-trimethyl­benzyl­idene]ethane-1,2-diamine
title N,N′-Bis[(E)-2,4,6-trimethyl­benzyl­idene]ethane-1,2-diamine
title_full N,N′-Bis[(E)-2,4,6-trimethyl­benzyl­idene]ethane-1,2-diamine
title_fullStr N,N′-Bis[(E)-2,4,6-trimethyl­benzyl­idene]ethane-1,2-diamine
title_full_unstemmed N,N′-Bis[(E)-2,4,6-trimethyl­benzyl­idene]ethane-1,2-diamine
title_short N,N′-Bis[(E)-2,4,6-trimethyl­benzyl­idene]ethane-1,2-diamine
title_sort n,n′-bis[(e)-2,4,6-trimethyl­benzyl­idene]ethane-1,2-diamine
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3213609/
https://www.ncbi.nlm.nih.gov/pubmed/22091186
http://dx.doi.org/10.1107/S1600536811029424
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AT betzrichard nnbise246trimethylbenzylideneethane12diamine

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